Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 20
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 30
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 62
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs2853676 0.667 0.560 5 1288432 intron variant T/A;C snv 23
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 32
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 46
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 36
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 135
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 98
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 264